Rheumatoid FactorTest Kit ( Nephelometry immunoassay Method) - FDA Registration 0917ff7aa2cf0e0e8ccf504b19dbbd54
Access comprehensive regulatory information for Rheumatoid FactorTest Kit ( Nephelometry immunoassay Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0917ff7aa2cf0e0e8ccf504b19dbbd54 and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on October 20, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
0917ff7aa2cf0e0e8ccf504b19dbbd54
Rheumatoid FactorTest Kit ( Nephelometry immunoassay Method)
FDA ID: 0917ff7aa2cf0e0e8ccf504b19dbbd54
Local name: Rheumatoid FactorTest Kit ๏ผ Nephelometry immunoassay Method๏ผ
Device Classification
Brand Name
Hiproโข
Registration Information
Analysis ID
0917ff7aa2cf0e0e8ccf504b19dbbd54
Registration Date
October 20, 2022
Manufacturer
Authorized Representative

